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FDA 510(k)

RelieVRx (Pico G3)

K-Number: K251519 · 2025-08-13

ApplicantAppliedvr
Decision Date2025-08-13
Product CodeQRA
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RelieVRx (Pico G3) is a medical device manufactured by Appliedvr. It received FDA 510(k) clearance on 2025-08-13 under approval number K251519. The device is classified under product code QRA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RelieVRx (Pico G3)?

RelieVRx (Pico G3) is a medical device that received FDA 510(k) clearance on 2025-08-13. It is manufactured by Appliedvr. The 510(k) number is K251519.

When was RelieVRx (Pico G3) approved by the FDA?

RelieVRx (Pico G3) received FDA 510(k) clearance on 2025-08-13, under approval number K251519.

What company makes RelieVRx (Pico G3)?

RelieVRx (Pico G3) is manufactured by Appliedvr.

What is the FDA product code for RelieVRx (Pico G3)?

The FDA product code for RelieVRx (Pico G3) is QRA.

Other Devices by Appliedvr

K243417RelieVRx

Related Devices (Code: QRA)

DEN210014EaseVRxAppliedvr, Inc. K230814VRNTCognifisense, Inc. K230825Smileyscope System (Therapy Mode)Smileyscope Holding, Inc. K243417RelieVRxAppliedvr K254004VRNTCognifisense, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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